CA3223825C - One-component moisture-curable adhesive composition - Google Patents
One-component moisture-curable adhesive composition Download PDFInfo
- Publication number
- CA3223825C CA3223825C CA3223825A CA3223825A CA3223825C CA 3223825 C CA3223825 C CA 3223825C CA 3223825 A CA3223825 A CA 3223825A CA 3223825 A CA3223825 A CA 3223825A CA 3223825 C CA3223825 C CA 3223825C
- Authority
- CA
- Canada
- Prior art keywords
- adhesive composition
- composition according
- component moisture
- curable adhesive
- isocyanate
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
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- 239000000203 mixture Substances 0.000 title claims abstract description 104
- 239000000853 adhesive Substances 0.000 title claims description 84
- 230000001070 adhesive effect Effects 0.000 title claims description 84
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims abstract description 41
- 235000010290 biphenyl Nutrition 0.000 claims abstract description 40
- 239000004305 biphenyl Substances 0.000 claims abstract description 40
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims abstract description 40
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 39
- 239000000463 material Substances 0.000 claims abstract description 37
- 150000003077 polyols Chemical class 0.000 claims abstract description 37
- 229920001228 polyisocyanate Polymers 0.000 claims abstract description 33
- 239000005056 polyisocyanate Substances 0.000 claims abstract description 33
- 229920005862 polyol Polymers 0.000 claims abstract description 33
- 239000004721 Polyphenylene oxide Substances 0.000 claims abstract description 30
- 229920000570 polyether Polymers 0.000 claims abstract description 30
- 239000002023 wood Substances 0.000 claims abstract description 27
- 229920005903 polyol mixture Polymers 0.000 claims abstract description 26
- 150000002009 diols Chemical class 0.000 claims abstract description 17
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims abstract description 16
- 150000001412 amines Chemical class 0.000 claims abstract description 15
- 125000005442 diisocyanate group Chemical group 0.000 claims abstract description 14
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical compound ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 claims abstract description 11
- 239000004839 Moisture curing adhesive Substances 0.000 claims abstract 2
- 238000001723 curing Methods 0.000 claims description 10
- 239000003054 catalyst Substances 0.000 claims description 9
- 238000000034 method Methods 0.000 claims description 7
- 239000000654 additive Substances 0.000 claims description 5
- 239000002518 antifoaming agent Substances 0.000 claims description 5
- 239000002562 thickening agent Substances 0.000 claims description 5
- 239000004793 Polystyrene Substances 0.000 claims description 3
- 229920002223 polystyrene Polymers 0.000 claims description 3
- 238000001542 size-exclusion chromatography Methods 0.000 claims description 3
- -1 aminoether polyol Chemical class 0.000 description 22
- 239000000047 product Substances 0.000 description 18
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 14
- 238000003825 pressing Methods 0.000 description 9
- 239000004814 polyurethane Substances 0.000 description 8
- 229920002635 polyurethane Polymers 0.000 description 8
- 238000013008 moisture curing Methods 0.000 description 7
- 230000000712 assembly Effects 0.000 description 6
- 238000000429 assembly Methods 0.000 description 6
- 239000012948 isocyanate Substances 0.000 description 6
- 150000002513 isocyanates Chemical class 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 238000004026 adhesive bonding Methods 0.000 description 4
- 230000032798 delamination Effects 0.000 description 4
- 230000002349 favourable effect Effects 0.000 description 4
- 239000003292 glue Substances 0.000 description 4
- 239000003960 organic solvent Substances 0.000 description 4
- 241000446313 Lamella Species 0.000 description 3
- 239000004743 Polypropylene Substances 0.000 description 3
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 3
- 239000003999 initiator Substances 0.000 description 3
- PGYPOBZJRVSMDS-UHFFFAOYSA-N loperamide hydrochloride Chemical compound Cl.C=1C=CC=CC=1C(C=1C=CC=CC=1)(C(=O)N(C)C)CCN(CC1)CCC1(O)C1=CC=C(Cl)C=C1 PGYPOBZJRVSMDS-UHFFFAOYSA-N 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 229920001155 polypropylene Polymers 0.000 description 3
- 229920000909 polytetrahydrofuran Polymers 0.000 description 3
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- ZMSQJSMSLXVTKN-UHFFFAOYSA-N 4-[2-(2-morpholin-4-ylethoxy)ethyl]morpholine Chemical compound C1COCCN1CCOCCN1CCOCC1 ZMSQJSMSLXVTKN-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 2
- 229920001730 Moisture cure polyurethane Polymers 0.000 description 2
- 241000218657 Picea Species 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000003475 lamination Methods 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 238000002791 soaking Methods 0.000 description 2
- HXKKHQJGJAFBHI-UHFFFAOYSA-N 1-aminopropan-2-ol Chemical compound CC(O)CN HXKKHQJGJAFBHI-UHFFFAOYSA-N 0.000 description 1
- BYACHAOCSIPLCM-UHFFFAOYSA-N 2-[2-[bis(2-hydroxyethyl)amino]ethyl-(2-hydroxyethyl)amino]ethanol Chemical compound OCCN(CCO)CCN(CCO)CCO BYACHAOCSIPLCM-UHFFFAOYSA-N 0.000 description 1
- HOSGXJWQVBHGLT-UHFFFAOYSA-N 6-hydroxy-3,4-dihydro-1h-quinolin-2-one Chemical group N1C(=O)CCC2=CC(O)=CC=C21 HOSGXJWQVBHGLT-UHFFFAOYSA-N 0.000 description 1
- 241000163925 Bembidion minimum Species 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- 240000000731 Fagus sylvatica Species 0.000 description 1
- 235000010099 Fagus sylvatica Nutrition 0.000 description 1
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 230000001588 bifunctional effect Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000011449 brick Substances 0.000 description 1
- 238000009435 building construction Methods 0.000 description 1
- 239000004566 building material Substances 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- VPKDCDLSJZCGKE-UHFFFAOYSA-N carbodiimide group Chemical group N=C=N VPKDCDLSJZCGKE-UHFFFAOYSA-N 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 239000008199 coating composition Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000004567 concrete Substances 0.000 description 1
- 229940043237 diethanolamine Drugs 0.000 description 1
- LVTYICIALWPMFW-UHFFFAOYSA-N diisopropanolamine Chemical compound CC(O)CNCC(C)O LVTYICIALWPMFW-UHFFFAOYSA-N 0.000 description 1
- 229940043276 diisopropanolamine Drugs 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 229940031098 ethanolamine Drugs 0.000 description 1
- 125000001033 ether group Chemical group 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 239000010440 gypsum Substances 0.000 description 1
- 229910052602 gypsum Inorganic materials 0.000 description 1
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexamethylene diamine Natural products NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 1
- VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical group C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 229940102253 isopropanolamine Drugs 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- CRVGTESFCCXCTH-UHFFFAOYSA-N methyl diethanolamine Chemical compound OCCN(C)CCO CRVGTESFCCXCTH-UHFFFAOYSA-N 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 150000002902 organometallic compounds Chemical class 0.000 description 1
- 239000000123 paper Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000011120 plywood Substances 0.000 description 1
- 239000003495 polar organic solvent Substances 0.000 description 1
- 229920001748 polybutylene Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 230000008646 thermal stress Effects 0.000 description 1
- 238000004078 waterproofing Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/74—Polyisocyanates or polyisothiocyanates cyclic
- C08G18/76—Polyisocyanates or polyisothiocyanates cyclic aromatic
- C08G18/7657—Polyisocyanates or polyisothiocyanates cyclic aromatic containing two or more aromatic rings
- C08G18/7664—Polyisocyanates or polyisothiocyanates cyclic aromatic containing two or more aromatic rings containing alkylene polyphenyl groups
- C08G18/7671—Polyisocyanates or polyisothiocyanates cyclic aromatic containing two or more aromatic rings containing alkylene polyphenyl groups containing only one alkylene bisphenyl group
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B21/00—Layered products comprising a layer of wood, e.g. wood board, veneer, wood particle board
- B32B21/04—Layered products comprising a layer of wood, e.g. wood board, veneer, wood particle board comprising wood as the main or only constituent of a layer, which is next to another layer of the same or of a different material
- B32B21/042—Layered products comprising a layer of wood, e.g. wood board, veneer, wood particle board comprising wood as the main or only constituent of a layer, which is next to another layer of the same or of a different material of wood
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B7/00—Layered products characterised by the relation between layers; Layered products characterised by the relative orientation of features between layers, or by the relative values of a measurable parameter between layers, i.e. products comprising layers having different physical, chemical or physicochemical properties; Layered products characterised by the interconnection of layers
- B32B7/04—Interconnection of layers
- B32B7/12—Interconnection of layers using interposed adhesives or interposed materials with bonding properties
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/08—Processes
- C08G18/10—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
- C08G18/12—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step using two or more compounds having active hydrogen in the first polymerisation step
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/08—Processes
- C08G18/16—Catalysts
- C08G18/18—Catalysts containing secondary or tertiary amines or salts thereof
- C08G18/20—Heterocyclic amines; Salts thereof
- C08G18/2081—Heterocyclic amines; Salts thereof containing at least two non-condensed heterocyclic rings
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/30—Low-molecular-weight compounds
- C08G18/302—Water
- C08G18/307—Atmospheric humidity
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/48—Polyethers
- C08G18/4804—Two or more polyethers of different physical or chemical nature
- C08G18/4812—Mixtures of polyetherdiols with polyetherpolyols having at least three hydroxy groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/48—Polyethers
- C08G18/4804—Two or more polyethers of different physical or chemical nature
- C08G18/482—Mixtures of polyethers containing at least one polyether containing nitrogen
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/48—Polyethers
- C08G18/4829—Polyethers containing at least three hydroxy groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/48—Polyethers
- C08G18/4854—Polyethers containing oxyalkylene groups having four carbon atoms in the alkylene group
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/77—Polyisocyanates or polyisothiocyanates having heteroatoms in addition to the isocyanate or isothiocyanate nitrogen and oxygen or sulfur
- C08G18/78—Nitrogen
- C08G18/79—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates
- C08G18/797—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates containing carbodiimide and/or uretone-imine groups
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J175/00—Adhesives based on polyureas or polyurethanes; Adhesives based on derivatives of such polymers
- C09J175/04—Polyurethanes
- C09J175/08—Polyurethanes from polyethers
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Laminated Bodies (AREA)
- Polyurethanes Or Polyureas (AREA)
Abstract
The invention relates to a one-component moisture-curing adhesive composition and its use for bonding a first piece of material to a second piece of material, such as in a structural wood product, the composition comprising from 80 to 100 wt% of an isocyanate-functional prepolymer obtainable by reacting: (a) a polyisocyanates mixture having an average nominal isocyanate functionality in the range of from above 2.00 to below 2.05 comprising: (al) a diisocyanate comprising methyl diphenyl diisocyanate; and (a2) an uretonimine-modified methyl diphenyl diisocyanate comprising at least 3 isocyanate functional groups; and (b) a polyol mixture comprising: (bl) a linear butylene oxide-based diol with two primary hydroxyl groups; (b2) a polyether triol with three secondary hydroxyl groups; and (b3) an amine-initiated polyether polyol.
Description
ONE-COMPONENT MOISTURE-CURABLE ADHESIVE COMPOSITION
Field of the Invention The present invention relates to a one-component moisture-curable adhesive .. composition comprising an isocyanate-functional prepolymer, to a method of bonding a first piece of material to a second piece of material using such adhesive composition and to an object comprising a first piece of material and a second piece of material bonded with such adhesive composition, in particular a structural wood product.
Background of the Invention Glued laminated timber, also called laminated timber beams, glue-laminated beams or glulam, is a structural timber product composed of several layers of dimensioned lumber glued together. By laminating several smaller pieces of wood, a single large, strong, structural member can be manufactured from smaller timbers, for example for use as ridge beams, garage door headers, floor beams, vertical columns, or horizontal beams, often in curved, arching shapes. Glued laminated beams are used in a wide range of applications in building construction. Another glued laminated wood product is cross-laminated timber (CLT), which is a wood panel product made by gluing layers of solid-sawn lumber together. Each layer of board is oriented perpendicular to adjacent layers and glued on the wide faces of each board, usually in a symmetric way so that the outer layers have the same orientation. Regular timber is an anisotropic material, meaning that the mechanical properties vary depending on the direction in which force is applied. By gluing layers of wood at perpendicular angles, the panel is able to achieve better structural rigidity in both directions. CLT is distinct to glued laminated timber, a product with all laminations oriented in the same way.
Adhesive compositions used in building materials such as glued laminated wood products and other structured wood products (also known as engineered wood products) need to meet stringent requirements with respect to adhesion strength
Field of the Invention The present invention relates to a one-component moisture-curable adhesive .. composition comprising an isocyanate-functional prepolymer, to a method of bonding a first piece of material to a second piece of material using such adhesive composition and to an object comprising a first piece of material and a second piece of material bonded with such adhesive composition, in particular a structural wood product.
Background of the Invention Glued laminated timber, also called laminated timber beams, glue-laminated beams or glulam, is a structural timber product composed of several layers of dimensioned lumber glued together. By laminating several smaller pieces of wood, a single large, strong, structural member can be manufactured from smaller timbers, for example for use as ridge beams, garage door headers, floor beams, vertical columns, or horizontal beams, often in curved, arching shapes. Glued laminated beams are used in a wide range of applications in building construction. Another glued laminated wood product is cross-laminated timber (CLT), which is a wood panel product made by gluing layers of solid-sawn lumber together. Each layer of board is oriented perpendicular to adjacent layers and glued on the wide faces of each board, usually in a symmetric way so that the outer layers have the same orientation. Regular timber is an anisotropic material, meaning that the mechanical properties vary depending on the direction in which force is applied. By gluing layers of wood at perpendicular angles, the panel is able to achieve better structural rigidity in both directions. CLT is distinct to glued laminated timber, a product with all laminations oriented in the same way.
Adhesive compositions used in building materials such as glued laminated wood products and other structured wood products (also known as engineered wood products) need to meet stringent requirements with respect to adhesion strength
2 under indoor and outdoor conditions. Exposure to moisture and thermal stress causes tension in the wood due to swelling and shrinkage and requires an adhesive that can provide superior bond strength even under such conditions.
One-component moisture-curing polyurethane adhesives are known for bonding pieces of wood to form structural wood products such as glued laminated wood products. Such adhesive compositions comprise an isocyanate-functional prepolymer that cures upon reacting with moisture. Isocyanate groups in the prepolymer react with water to form amine groups that react with further isocyanate groups to form urea bonds. When used for manufacturing glued structural wood products, the adhesive composition is typically applied on a surface of a piece of wood, such as timber or lumber, and then different pieces of wood are pressed together to cure the adhesive composition and form a structural wood product.
Such polyurethane adhesives are for example described in WO 99/19141, US 2005/032972, and WO 2021/022470.
In WO 99/19141 is described a polyisocyanate adhesive for use in lignocellulosic-based structural lamination manufacture (plywood manufacture). The adhesive comprises an isocyanate-containing prepolymer having an isocyanate content of 5 to 25% obtainable by reacting a polyol mixture with an average nominal functionality of from 2 to 4 and an average equivalent weight of from 500 to 3000, with a stoichiometric excess of methyl diphenyl di isocyanate. Polypropylene-polyethylene-oxide polyols with up to 5 % of another polyol are mentioned as particularly preferred polyol mixtures.
In US 2005/032972 is described a fast setting one-pack polyurethane adhesive containing a polyisocyanate prepolymer and at least one aminoether polyol, having a molar ratio of ether groups to amino nitrogen in the aminopolyether polyol of 7 to 30.
.. The polyurethane prepolymer is produced by reaction of polyisocyanates with compounds containing isocyanate-reactive functional groups.
One-component moisture-curing polyurethane adhesives are known for bonding pieces of wood to form structural wood products such as glued laminated wood products. Such adhesive compositions comprise an isocyanate-functional prepolymer that cures upon reacting with moisture. Isocyanate groups in the prepolymer react with water to form amine groups that react with further isocyanate groups to form urea bonds. When used for manufacturing glued structural wood products, the adhesive composition is typically applied on a surface of a piece of wood, such as timber or lumber, and then different pieces of wood are pressed together to cure the adhesive composition and form a structural wood product.
Such polyurethane adhesives are for example described in WO 99/19141, US 2005/032972, and WO 2021/022470.
In WO 99/19141 is described a polyisocyanate adhesive for use in lignocellulosic-based structural lamination manufacture (plywood manufacture). The adhesive comprises an isocyanate-containing prepolymer having an isocyanate content of 5 to 25% obtainable by reacting a polyol mixture with an average nominal functionality of from 2 to 4 and an average equivalent weight of from 500 to 3000, with a stoichiometric excess of methyl diphenyl di isocyanate. Polypropylene-polyethylene-oxide polyols with up to 5 % of another polyol are mentioned as particularly preferred polyol mixtures.
In US 2005/032972 is described a fast setting one-pack polyurethane adhesive containing a polyisocyanate prepolymer and at least one aminoether polyol, having a molar ratio of ether groups to amino nitrogen in the aminopolyether polyol of 7 to 30.
.. The polyurethane prepolymer is produced by reaction of polyisocyanates with compounds containing isocyanate-reactive functional groups.
3 In WO 2021/022470 is described a one-component polyurethane prepolymer composition for waterproofing coating applications. It comprises a reaction product of at least one polyisocyanate and a polyol blend comprising a bifunctional polyether polyol with a weight average molecular weight from 3,000 to 9,000 g/mol and a trifunctional polyether polyol end-capped with 10-28 wt% of ethylene oxide and a weight average molecular weight from 5,000 to 8,000 g/mol.
The balance between maximum assembly time (AT) and minimum pressing time (PT) is very important for one-component moisture-curing polyurethane adhesive compositions. Maximum assembly time is the time pieces of material with adhesive composition applied on it can be assembled before pressing. The applied adhesive composition still needs to be curable when the pieces are pressed together.
Minimum pressing time is the time in the press needed to give enough bonding of the pressed pieces of material to allow further processing of the structural product. A
ratio of AT to PT of 1:1 to 1:2.5 is often acceptable. Ideally, the AT/PT ratio is close to 1.1, preferably between 1:1 and 1:2, more preferably between 1:1 and 1:2. Adhesive compositions with a very good AT/PT ratio are typically poorer in mechanical properties such as wet and dry adhesion strength compared to products with a less favourable AT/PT ratio. Therefore, fibres are often added to one-component moisture-curing polyurethane adhesive compositions to improve mechanical properties such as longitudinal tensile strength.
There is a need in the art for one-component moisture-curing polyurethane adhesive compositions that combine a favourable AT/PT ratio with good mechanical properties even without fibres.
Summary of the Invention It has now been found that a one-component moisture-curable adhesive composition comprising an isocyanate-functional prepolymer provides good adhesion and has a favourable AT/PT ratio if the prepolymer is prepared by reacting excess
The balance between maximum assembly time (AT) and minimum pressing time (PT) is very important for one-component moisture-curing polyurethane adhesive compositions. Maximum assembly time is the time pieces of material with adhesive composition applied on it can be assembled before pressing. The applied adhesive composition still needs to be curable when the pieces are pressed together.
Minimum pressing time is the time in the press needed to give enough bonding of the pressed pieces of material to allow further processing of the structural product. A
ratio of AT to PT of 1:1 to 1:2.5 is often acceptable. Ideally, the AT/PT ratio is close to 1.1, preferably between 1:1 and 1:2, more preferably between 1:1 and 1:2. Adhesive compositions with a very good AT/PT ratio are typically poorer in mechanical properties such as wet and dry adhesion strength compared to products with a less favourable AT/PT ratio. Therefore, fibres are often added to one-component moisture-curing polyurethane adhesive compositions to improve mechanical properties such as longitudinal tensile strength.
There is a need in the art for one-component moisture-curing polyurethane adhesive compositions that combine a favourable AT/PT ratio with good mechanical properties even without fibres.
Summary of the Invention It has now been found that a one-component moisture-curable adhesive composition comprising an isocyanate-functional prepolymer provides good adhesion and has a favourable AT/PT ratio if the prepolymer is prepared by reacting excess
4 polyisocyanates comprising methyl diphenyl diisocyanate and uretonimine-modified methyl diphenyl diisocyanate with a specific polyol mixture, and if the content of free isocyanate groups in the adhesive composition is in the range of from 14 to 17 wt%.
Accordingly, the invention provides in a first aspect a one-component moisture-curing polyurethane adhesive cornposition comprising an isocyanate-functional prepolymer obtainable by reacting:
(a) a polyisocyanates mixture having an average nominal isocyanate functionality in the range of from above 2.00 to below 2.05 comprising:
(al) a diisocyanate comprising methyl diphenyl diisocyanate; and (a2) an uretonimine-modified methyl diphenyl diisocyanate comprising at least 3 isocyanate functional groups; and (b) a polyol mixture comprising (bl ) a linear butylene oxide-based diol with two primary hydroxyl groups;
(b2) a polyether triol with three secondary hydroxyl groups; and (b3) an amine-initiated polyether polyol;
wherein the equivalent ratio between isocyanate groups in (a) and hydroxyl groups in (b) is in the range of from 3.5 to 7.0, wherein the content of free isocyanate groups in the adhesive composition is in the range of from 14 to 17 wt%.
Due to its excellent adhesion properties and its favourable AT/PT ratio, the one-corn ponent moisture-curing polyurethane adhesive composition according to the first aspect is particularly suitable for bonding pieces of material, in particular pieces of wood such as lumber or timber to form structural wood products.
Accordingly, in a second aspect, the invention provides a method for bonding a first piece of material to a second piece of material, comprising contacting a surface of the first material with a surface of the second material, wherein at least one of the contacted surfaces has the adhesive composition according to the first aspect of the invention applied to it prior to the contacting.
In a final aspect, the invention provides an object comprising a first piece of material and a second piece of material bonded with the adhesive composition according to the second aspect of the invention, in particular a structural wood product.
Accordingly, the invention provides in a first aspect a one-component moisture-curing polyurethane adhesive cornposition comprising an isocyanate-functional prepolymer obtainable by reacting:
(a) a polyisocyanates mixture having an average nominal isocyanate functionality in the range of from above 2.00 to below 2.05 comprising:
(al) a diisocyanate comprising methyl diphenyl diisocyanate; and (a2) an uretonimine-modified methyl diphenyl diisocyanate comprising at least 3 isocyanate functional groups; and (b) a polyol mixture comprising (bl ) a linear butylene oxide-based diol with two primary hydroxyl groups;
(b2) a polyether triol with three secondary hydroxyl groups; and (b3) an amine-initiated polyether polyol;
wherein the equivalent ratio between isocyanate groups in (a) and hydroxyl groups in (b) is in the range of from 3.5 to 7.0, wherein the content of free isocyanate groups in the adhesive composition is in the range of from 14 to 17 wt%.
Due to its excellent adhesion properties and its favourable AT/PT ratio, the one-corn ponent moisture-curing polyurethane adhesive composition according to the first aspect is particularly suitable for bonding pieces of material, in particular pieces of wood such as lumber or timber to form structural wood products.
Accordingly, in a second aspect, the invention provides a method for bonding a first piece of material to a second piece of material, comprising contacting a surface of the first material with a surface of the second material, wherein at least one of the contacted surfaces has the adhesive composition according to the first aspect of the invention applied to it prior to the contacting.
In a final aspect, the invention provides an object comprising a first piece of material and a second piece of material bonded with the adhesive composition according to the second aspect of the invention, in particular a structural wood product.
5 Detailed Description of the Invention The adhesive composition according to the invention is a one-component, moisture-curable composition. It comprises an isocyanate-functional prepolymer, preferably in an amount of at least 80 wt%, more preferably at least 85 wt%, even more preferably at least 90 wt%. The adhesive composition may comprise the isocyanate-functional prepolymer in an amount up to 100 wt%, preferably up to 99.8 wt%.
The isocyanate-functional prepolymer is obtainable by reacting:
(a) a polyisocyanates mixture having an average nominal isocyanate functionality in the range of from above 2.00 to below 2.05 comprising:
(al) a diisocyanate comprising methyl diphenyl diisocyanate; and (a2) an uretonimine-modified methyl diphenyl diisocyanate comprising at least 3 isocyanate functional groups; and (b) a polyol mixture comprising (LA) a linear butylene oxide-based diol with two primary hydroxyl groups;
(b2) a polyether triol with three secondary hydroxyl groups; and (b3) an amine-initiated polyol;
wherein the equivalent ratio between isocyanate groups in (a) and hydroxyl groups in (b) is in the range of from 3.5 to 7Ø
Polyisocyanate mixture (a) comprises a diisocyanate (al) comprising methyl diphenyl diisocyanate and an uretomine-modified methyl diphenyl diisocyanate (a2) comprising at least 3 isocyanate functional groups. Polyisocyanate mixture (a) comprises diisocyanate (al) in excess of uretomine-modified methyl diphenyl diisocyanate (a2). The average nominal isocyanate functionality of polyisocyanates mixture (a) is in the range of from above 2.00 to below 2.05, preferably of from above
The isocyanate-functional prepolymer is obtainable by reacting:
(a) a polyisocyanates mixture having an average nominal isocyanate functionality in the range of from above 2.00 to below 2.05 comprising:
(al) a diisocyanate comprising methyl diphenyl diisocyanate; and (a2) an uretonimine-modified methyl diphenyl diisocyanate comprising at least 3 isocyanate functional groups; and (b) a polyol mixture comprising (LA) a linear butylene oxide-based diol with two primary hydroxyl groups;
(b2) a polyether triol with three secondary hydroxyl groups; and (b3) an amine-initiated polyol;
wherein the equivalent ratio between isocyanate groups in (a) and hydroxyl groups in (b) is in the range of from 3.5 to 7Ø
Polyisocyanate mixture (a) comprises a diisocyanate (al) comprising methyl diphenyl diisocyanate and an uretomine-modified methyl diphenyl diisocyanate (a2) comprising at least 3 isocyanate functional groups. Polyisocyanate mixture (a) comprises diisocyanate (al) in excess of uretomine-modified methyl diphenyl diisocyanate (a2). The average nominal isocyanate functionality of polyisocyanates mixture (a) is in the range of from above 2.00 to below 2.05, preferably of from above
6 2.00 to 2.04, more preferably of from above 2.00 to below 2.03. Typically, the average nominal isocyanate functionality of polyisocyanates mixture (a) is above 2.001; preferably above 2.002; more preferably above 2.003; still more preferably above 2.004; most preferably above 2.005. Reference herein to the average nominal isocyanate functionality is to the number average of isocyanate groups per molecule.
Diisocyanate (al) comprises methyl diphenyl diisocyanate (MDI). The methyl diphenyl diisocyanate may be 4,4'-methyl diphenyl diisocyanate, 2,4'-methyl diphenyl diisocyanate, 2,2'-methyl diphenyl diisocyanate, or a mixture of two or more thereof.
Preferably, diisocyanate (al) consists of methyl diphenyl diisocyanate, more preferably consists of 4,4'-methyl diphenyl diisocyanate or of a mixture of 4,4'-methyl diphenyl diisocyanate and 2,4'-methyl diphenyl diisocyanate, and/or 2,2'-methyl diphenyl diisocyanate. Preferably the 4,4'-methyl diphenyl diisocyanate content of the polyisocyanate mixture (a) is in the range of from 50 to 100 wt%. Such mixtures are commercially available, for example as SuprasecTM 2004, SuprasecTM 6004 (ex.
Huntsman), LupranateTM MX 119/1 (ex. BASF), CosmoriateTM JG-50K, CosmonateTM
PI (ex. Kumho Mitsui Chemicals), or OngronatTM C04050 (ex. Wanhua).
For the purpose of this specification, the term methyl diphenyl diisocyanate refers to methyl diphenyl diisocyanate as such and does not include polymeric, oligomeric, or modified methyl diphenyl diisocyanate, such as for example carbodiimide-, uretonimine-, or isocyanurate-modified methyl diphenyl diisocyanate.
Uretonimine-modified methyl diphenyl diisocyanate (a2) comprises at least 3 isocyanate functional groups, preferably in the range of from 3 to 10 isocyanate functional groups, more preferably in the range of from 3 to 6 isocyanate functional groups, even more preferably 3 or 4 isocyanate functional groups.
Polyisocyanate mixture (a) may comprise polyisocyanate other than methyl diphenyl diisocyanate or uretonimine-modified methyl diphenyl diisocyanate, preferably in an amount up to 25 wt% of the total weight of polyisocyanates (a), more preferably up to Date Recue/Date Received 2024-03-11
Diisocyanate (al) comprises methyl diphenyl diisocyanate (MDI). The methyl diphenyl diisocyanate may be 4,4'-methyl diphenyl diisocyanate, 2,4'-methyl diphenyl diisocyanate, 2,2'-methyl diphenyl diisocyanate, or a mixture of two or more thereof.
Preferably, diisocyanate (al) consists of methyl diphenyl diisocyanate, more preferably consists of 4,4'-methyl diphenyl diisocyanate or of a mixture of 4,4'-methyl diphenyl diisocyanate and 2,4'-methyl diphenyl diisocyanate, and/or 2,2'-methyl diphenyl diisocyanate. Preferably the 4,4'-methyl diphenyl diisocyanate content of the polyisocyanate mixture (a) is in the range of from 50 to 100 wt%. Such mixtures are commercially available, for example as SuprasecTM 2004, SuprasecTM 6004 (ex.
Huntsman), LupranateTM MX 119/1 (ex. BASF), CosmoriateTM JG-50K, CosmonateTM
PI (ex. Kumho Mitsui Chemicals), or OngronatTM C04050 (ex. Wanhua).
For the purpose of this specification, the term methyl diphenyl diisocyanate refers to methyl diphenyl diisocyanate as such and does not include polymeric, oligomeric, or modified methyl diphenyl diisocyanate, such as for example carbodiimide-, uretonimine-, or isocyanurate-modified methyl diphenyl diisocyanate.
Uretonimine-modified methyl diphenyl diisocyanate (a2) comprises at least 3 isocyanate functional groups, preferably in the range of from 3 to 10 isocyanate functional groups, more preferably in the range of from 3 to 6 isocyanate functional groups, even more preferably 3 or 4 isocyanate functional groups.
Polyisocyanate mixture (a) may comprise polyisocyanate other than methyl diphenyl diisocyanate or uretonimine-modified methyl diphenyl diisocyanate, preferably in an amount up to 25 wt% of the total weight of polyisocyanates (a), more preferably up to Date Recue/Date Received 2024-03-11
7 wt%. In a particularly preferred embodiment, the polyisocyanate mixture (a) consists of methyl diphenyl diisocyanate and uretonimine-modified methyl diphenyl diisocyanate and is free of any other polyisocyanate.
Polyol mixture (b) comprises a linear butylene oxide-based diol with two primary 5 hydroxyl groups (b1), a polyether trial with three secondary hydroxyl groups (b2) and an amine-initiated polyol (b3).
Butylene oxide-based dial (b1) is linear and has two primary hydroxyl groups.
The two primary hydroxyl groups are terminal hydroxyl groups. Such dials can be 10 obtained by polymerizing butylene oxide, also known as tetrahydrofuran, and are also known as poly(tetrahydrofuran), poly(tetramethylene ether)glycol, poly(tetramethylene oxide), or poly(1,4-butanediol). Preferably, diol (b1) has a number average molecular weight in the range of from 500 to 2,500 g/mol, more preferably of from 500 to 1,500 g/mol. Such dials (b1) are commercially available, for example as PolyTHFTm 650, PolyTHFTm 1000, PolyTHFTm 1400 (ex. BASF).
Polyether trial (b2) has three secondary hydroxyl groups. Polyether trial (b2) preferably is a polyethylene ether, a polypropylene ether, a polybutylene ether, or a hybrid thereof, more preferably a polyethylene ether, a polypropylene ether or a hybrid thereof. Preferably, polyether trio! (b2) has a number average molecular weight in the range of from 500 to 2,500 g/mol, more preferably of from 500 to 1,500 g/mol. An example of a particularly suitable polyether trial (b2) is VoranolTM
(commercially available from Dow), a polypropylene ether triol with a number average molecular weight of 1,000 g/mol.
Amine-initiated polyether polyol (b3) is a polyol prepared by using an amine as an initiator molecule, preferably an aliphatic amine. Suitable amine initiator molecules include ethylene diamine hexamethylene diamine, methyl amine, isopropanolamine, diisopropanolamine, ethanolamine, diethanolamine, N-methyl diethanolamine, tetrahydroxyethyl ethylenediamine, or mixtures thereof. The amine initiator preferably contains Ito 18 carbon atoms, more preferably Ito 6 carbon atoms. The amine-Date Recue/Date Received 2024-03-11
Polyol mixture (b) comprises a linear butylene oxide-based diol with two primary 5 hydroxyl groups (b1), a polyether trial with three secondary hydroxyl groups (b2) and an amine-initiated polyol (b3).
Butylene oxide-based dial (b1) is linear and has two primary hydroxyl groups.
The two primary hydroxyl groups are terminal hydroxyl groups. Such dials can be 10 obtained by polymerizing butylene oxide, also known as tetrahydrofuran, and are also known as poly(tetrahydrofuran), poly(tetramethylene ether)glycol, poly(tetramethylene oxide), or poly(1,4-butanediol). Preferably, diol (b1) has a number average molecular weight in the range of from 500 to 2,500 g/mol, more preferably of from 500 to 1,500 g/mol. Such dials (b1) are commercially available, for example as PolyTHFTm 650, PolyTHFTm 1000, PolyTHFTm 1400 (ex. BASF).
Polyether trial (b2) has three secondary hydroxyl groups. Polyether trial (b2) preferably is a polyethylene ether, a polypropylene ether, a polybutylene ether, or a hybrid thereof, more preferably a polyethylene ether, a polypropylene ether or a hybrid thereof. Preferably, polyether trio! (b2) has a number average molecular weight in the range of from 500 to 2,500 g/mol, more preferably of from 500 to 1,500 g/mol. An example of a particularly suitable polyether trial (b2) is VoranolTM
(commercially available from Dow), a polypropylene ether triol with a number average molecular weight of 1,000 g/mol.
Amine-initiated polyether polyol (b3) is a polyol prepared by using an amine as an initiator molecule, preferably an aliphatic amine. Suitable amine initiator molecules include ethylene diamine hexamethylene diamine, methyl amine, isopropanolamine, diisopropanolamine, ethanolamine, diethanolamine, N-methyl diethanolamine, tetrahydroxyethyl ethylenediamine, or mixtures thereof. The amine initiator preferably contains Ito 18 carbon atoms, more preferably Ito 6 carbon atoms. The amine-Date Recue/Date Received 2024-03-11
8 initiated polyether polyol (b3) is a polyether, preferably a poly(ethylene oxide),a poly(propylene oxide) or a hybrid thereof. Amine-initiated polyether polyol (b3) preferably contains 2 to 6 hydroxyl groups, more preferably 2 to 4 hydroxyl groups, even more preferably 3 or 4 hydroxyl groups. The number average molecular weight of amine-initiated polyether polyol (b3) is preferably in the range of from 1,000 to 10,000 g/mol, more preferably of from 1,000 to 6,000 g/mol, even more preferably of from 1,500 to 5,000 g/mol. Preferably, at least part of the hydroxyl groups are primary hydroxyl groups. Primary hydroxyl groups may be obtained by end-capping the polyether chains with ethylene oxide. Such amine-initiated polyether polyols are commercially available, for example LupranolTM 1002/1 (ex. BASF).
Typically, the amount of butylene oxide-based diol (b1) in polyol mixture (b) is such that in the range of from 45 to 85% of the hydroxyl groups in polyol mixture (b) are hydroxyl groups from butylene oxide-based diol (b1), preferably in the range of from 50 to 80%, more preferably from 55 to 75%, most preferably from 60 to 70%. It has been found that a content of hydroxyl groups from butylene oxide-based diol (b1) in polyol mixture (b) in the range of from 55 to 75% improves the AT/PT ratio compared to lower contents.
Typically, the amount of polyether triol (b2) in polyol mixture (b) is such that in the range of 20 to 70% of the hydroxyl groups in polyol mixture (b) are hydroxyl groups from polyether triol (b2), preferably, from 30 to 60%, more preferably from 35 to 55%.
Polyol mixture (b) may comprise polyols other than butylene oxide-based diol (bl) and polyether triol (b2), preferably in an amount less than 50 wt% of polyol mixture (b), more preferably less than 30 wt%, even more preferably less than 10 wt%.
In a particularly preferred embodiment, polyol mixture (b) is substantially free of any polyols other than (b1) and (b2). Reference herein to substantially free of any polyols other than (b1) and (b2) is to the polyol mixture comprising at most 1 wt% of any polyols other than (b1) and (b2), preferably at most 0.5 wt%, even more preferably to a polyol mixture free of any polyols other than (b1) and (b2).
Date Recue/Date Received 2024-03-11
Typically, the amount of butylene oxide-based diol (b1) in polyol mixture (b) is such that in the range of from 45 to 85% of the hydroxyl groups in polyol mixture (b) are hydroxyl groups from butylene oxide-based diol (b1), preferably in the range of from 50 to 80%, more preferably from 55 to 75%, most preferably from 60 to 70%. It has been found that a content of hydroxyl groups from butylene oxide-based diol (b1) in polyol mixture (b) in the range of from 55 to 75% improves the AT/PT ratio compared to lower contents.
Typically, the amount of polyether triol (b2) in polyol mixture (b) is such that in the range of 20 to 70% of the hydroxyl groups in polyol mixture (b) are hydroxyl groups from polyether triol (b2), preferably, from 30 to 60%, more preferably from 35 to 55%.
Polyol mixture (b) may comprise polyols other than butylene oxide-based diol (bl) and polyether triol (b2), preferably in an amount less than 50 wt% of polyol mixture (b), more preferably less than 30 wt%, even more preferably less than 10 wt%.
In a particularly preferred embodiment, polyol mixture (b) is substantially free of any polyols other than (b1) and (b2). Reference herein to substantially free of any polyols other than (b1) and (b2) is to the polyol mixture comprising at most 1 wt% of any polyols other than (b1) and (b2), preferably at most 0.5 wt%, even more preferably to a polyol mixture free of any polyols other than (b1) and (b2).
Date Recue/Date Received 2024-03-11
9 Preferably, the amount of amine-initiated polyether polyol (b3) in polyol mixture (b) is such that the number of hydroxyl groups from amine-initiated polyether polyol (b3) is at most 50%, preferably at most 40%, even more preferably at most 20%, still more preferably at most 15% of the total number of hydroxyl groups in polyol mixture (b).
The amount of butylene oxide-based diol (b1) in polyol mixture (b) is preferably such that the number of hydroxyl groups from butylene oxide-based diol (b1) is at least 40% of the total number of hydroxyl groups in polyol mixture (b).
The isocyanate-functional prepolymer is obtainable by reacting excess polyisocyanate with polyols. The equivalent ratio of isocyanate groups in the polyisocyanate mixture (a) and hydroxyl groups in polyol mixture (b) is in the range of from 3.5 to 7.0, preferably in the range of from 4.0 to 6.5, more preferably of from 4.5 to 6Ø A larger excess of polyisocyanate might result in a lower molecular weight of the resulting prepolymer, which might negatively affect bonding strength and AT/PT
ratio.
Preferably, the isocyanate-functional prepolymer has a weight average molecular weight of at least 1,500 g/mol, more preferably of at least 2,000 g/mole. A
weight average molecular weight in the range of from 2,000 to 5,000 g/mol is particularly preferred.
Reaction conditions for preparing isocyanate-functional prepolymer from polyisocyanate and polyol are well-known in the art. Any suitable reaction conditions may be used.
Reference herein to number average molecular weight or weight average molecular weight is to the number average molecular weight or the weight average molecular weight as determined by size-exclusion chromatography using polystyrene standards. A suitable determination method is ISO 16014-1.
The adhesive composition may comprise components other than the isocyanate-functional prepolymer, such as for example organic solvent, reactive diluent, curing catalyst, pigments, fillers, and one or more additives, such as defoaming agents and thickeners.
The adhesive composition may comprise organic solvent, preferably in an amount of at most 10 wt% of the total weight of the adhesive composition, more preferably at most 5 wt%, even more preferably at most 2 wt%. If an organic solvent is present, the organic solvent preferably is a polar organic solvent such as for example a ketone, an
The amount of butylene oxide-based diol (b1) in polyol mixture (b) is preferably such that the number of hydroxyl groups from butylene oxide-based diol (b1) is at least 40% of the total number of hydroxyl groups in polyol mixture (b).
The isocyanate-functional prepolymer is obtainable by reacting excess polyisocyanate with polyols. The equivalent ratio of isocyanate groups in the polyisocyanate mixture (a) and hydroxyl groups in polyol mixture (b) is in the range of from 3.5 to 7.0, preferably in the range of from 4.0 to 6.5, more preferably of from 4.5 to 6Ø A larger excess of polyisocyanate might result in a lower molecular weight of the resulting prepolymer, which might negatively affect bonding strength and AT/PT
ratio.
Preferably, the isocyanate-functional prepolymer has a weight average molecular weight of at least 1,500 g/mol, more preferably of at least 2,000 g/mole. A
weight average molecular weight in the range of from 2,000 to 5,000 g/mol is particularly preferred.
Reaction conditions for preparing isocyanate-functional prepolymer from polyisocyanate and polyol are well-known in the art. Any suitable reaction conditions may be used.
Reference herein to number average molecular weight or weight average molecular weight is to the number average molecular weight or the weight average molecular weight as determined by size-exclusion chromatography using polystyrene standards. A suitable determination method is ISO 16014-1.
The adhesive composition may comprise components other than the isocyanate-functional prepolymer, such as for example organic solvent, reactive diluent, curing catalyst, pigments, fillers, and one or more additives, such as defoaming agents and thickeners.
The adhesive composition may comprise organic solvent, preferably in an amount of at most 10 wt% of the total weight of the adhesive composition, more preferably at most 5 wt%, even more preferably at most 2 wt%. If an organic solvent is present, the organic solvent preferably is a polar organic solvent such as for example a ketone, an
10 ester, or an ether.
The adhesive composition may comprise a curing catalyst for curing the moisture-curing reaction, typically in an amount in the range of from 0 to 0.4 wt%.
Suitable curing catalysts are known in the art. Tertiary amines, organometallic compounds, and strong bases, are known to be suitable as curing catalyst. A particularly preferred curing catalyst is 2,2'-dimorpholinediethylether (DMDEE).
The adhesive composition may comprise any suitable additive commonly used in adhesion compositions, such as for example defoaming agents, thickeners, and/or wetting agents. Preferably, the adhesive composition comprises a defoaming agent and/or a thickener.
The adhesive composition has a content of free isocyanate groups in the range of from 14 to 17 wt%, based on the total weight of the adhesive composition. Free isocyanate groups are free isocyanate groups in the prepolymer and any unreacted polyisocyanate monomers. Further polyisocyanate, preferably a diisocyanate, more preferably methyl diphenyl diisocyanate, may be added to the prepolymer to arrive at a content of free isocyanate groups in the adhesive composition in the range of from 14 to 17wt%.
More preferably, the adhesive composition has a content of free isocyanate groups in
The adhesive composition may comprise a curing catalyst for curing the moisture-curing reaction, typically in an amount in the range of from 0 to 0.4 wt%.
Suitable curing catalysts are known in the art. Tertiary amines, organometallic compounds, and strong bases, are known to be suitable as curing catalyst. A particularly preferred curing catalyst is 2,2'-dimorpholinediethylether (DMDEE).
The adhesive composition may comprise any suitable additive commonly used in adhesion compositions, such as for example defoaming agents, thickeners, and/or wetting agents. Preferably, the adhesive composition comprises a defoaming agent and/or a thickener.
The adhesive composition has a content of free isocyanate groups in the range of from 14 to 17 wt%, based on the total weight of the adhesive composition. Free isocyanate groups are free isocyanate groups in the prepolymer and any unreacted polyisocyanate monomers. Further polyisocyanate, preferably a diisocyanate, more preferably methyl diphenyl diisocyanate, may be added to the prepolymer to arrive at a content of free isocyanate groups in the adhesive composition in the range of from 14 to 17wt%.
More preferably, the adhesive composition has a content of free isocyanate groups in
11 the range of from 15.0 to 16.5 wt%.
The content of free isocyanate groups is determined according to ASTM D2572-19.
The adhesive composition preferably contains no or only trace amounts of water.
Preferably, the adhesive composition contains less than 1.0 wt%, more preferably less than 0.2 wt%, even more preferably less than 0.01 wt% of water, based on the total weight of the adhesive composition. Water is not explicitly added, e.g. to adjust the viscosity of the coating composition, but merely present, if at all, in trace amounts as part of typical adhesive additives.
The adhesive composition is preferably free of fibres.
In a preferred embodiment, the adhesive composition is free of any compounds other than the isocyanate-functional prepolymer, additional polyisocyanate, curing catalyst, and additives.
The one-component moisture-curable adhesive composition is particularly suitable for bonding pieces of wood or other materials to form structural products.
The invention therefore provides a method of bonding a first piece of material to a second piece of material, comprising contacting a surface of the first material with a surface of the second material, wherein at least one of the contacted surfaces has the adhesive composition according to the first aspect of the invention applied to it prior to the contacting.
In a third aspect, the invention provides an object comprising a first piece of material and a second piece of material bonded with the adhesive composition according to the first aspect of the invention.
The content of free isocyanate groups is determined according to ASTM D2572-19.
The adhesive composition preferably contains no or only trace amounts of water.
Preferably, the adhesive composition contains less than 1.0 wt%, more preferably less than 0.2 wt%, even more preferably less than 0.01 wt% of water, based on the total weight of the adhesive composition. Water is not explicitly added, e.g. to adjust the viscosity of the coating composition, but merely present, if at all, in trace amounts as part of typical adhesive additives.
The adhesive composition is preferably free of fibres.
In a preferred embodiment, the adhesive composition is free of any compounds other than the isocyanate-functional prepolymer, additional polyisocyanate, curing catalyst, and additives.
The one-component moisture-curable adhesive composition is particularly suitable for bonding pieces of wood or other materials to form structural products.
The invention therefore provides a method of bonding a first piece of material to a second piece of material, comprising contacting a surface of the first material with a surface of the second material, wherein at least one of the contacted surfaces has the adhesive composition according to the first aspect of the invention applied to it prior to the contacting.
In a third aspect, the invention provides an object comprising a first piece of material and a second piece of material bonded with the adhesive composition according to the first aspect of the invention.
12 The material may be any suitable material such as wood, metal, plastic, paper, glass, concrete, gypsum or other mineral material such as stone or brick. The first and the second pieces of material may be different materials. Preferably, the pieces of material are pieces of wood.
The object may be any suitable object. Preferably the material is wood, and the object is a structural wood product.
The invention is further illustrated by means of the following non-limiting examples.
Examples The polyisocyanates and polyols used in the examples are given in Table 1.
Table 1 Polyisocyanates and polyols used Commercial name Description Suprasec TM 2004 (ex. Huntsman) Mixture of 4,4-MDI, 2,4-MDI and 2,2-MDI;
nominal isocyanate functionality 2.0 Suprasec TM 2020 (ex. Huntsman) Mixture of MDI and uretonimine-modified MDI
with 3 NCO groups; average nominal isocyanate functionality 2.1 PolyTHFTm 1000 (ex. BASF) Poly(tetrahydrofuran); Mn is 1,000 g/mol VoranolTM CP1050 (ex. Dow) Glycerine initiated propoxylated polyether homopolymer triol; nominal hydroxyl functionality 3. Secondary hydroxyl groups. Mn is 1,078 g/mol.
LupranolTM 1002/1 (ex. BASF) Alkoxylate on the basis of an aliphatic amine. It contains primary hydroxyl end groups. Molecular weight is about 3,700 g/mol.
LupranolTM 2095 (ex. BASF) Trifunctional polyether polyol;
contains primary hydroxyl groups Preparation of isocvanate-functional prepolvmer Polyisocyanates and polyols were added to a three-neck reactor equipped with a mechanical stirrer and a cooler, under a nitrogen blanket. The amounts and type as Date Recue/Date Received 2024-03-11
The object may be any suitable object. Preferably the material is wood, and the object is a structural wood product.
The invention is further illustrated by means of the following non-limiting examples.
Examples The polyisocyanates and polyols used in the examples are given in Table 1.
Table 1 Polyisocyanates and polyols used Commercial name Description Suprasec TM 2004 (ex. Huntsman) Mixture of 4,4-MDI, 2,4-MDI and 2,2-MDI;
nominal isocyanate functionality 2.0 Suprasec TM 2020 (ex. Huntsman) Mixture of MDI and uretonimine-modified MDI
with 3 NCO groups; average nominal isocyanate functionality 2.1 PolyTHFTm 1000 (ex. BASF) Poly(tetrahydrofuran); Mn is 1,000 g/mol VoranolTM CP1050 (ex. Dow) Glycerine initiated propoxylated polyether homopolymer triol; nominal hydroxyl functionality 3. Secondary hydroxyl groups. Mn is 1,078 g/mol.
LupranolTM 1002/1 (ex. BASF) Alkoxylate on the basis of an aliphatic amine. It contains primary hydroxyl end groups. Molecular weight is about 3,700 g/mol.
LupranolTM 2095 (ex. BASF) Trifunctional polyether polyol;
contains primary hydroxyl groups Preparation of isocvanate-functional prepolvmer Polyisocyanates and polyols were added to a three-neck reactor equipped with a mechanical stirrer and a cooler, under a nitrogen blanket. The amounts and type as Date Recue/Date Received 2024-03-11
13 indicated in Table 2. The reactor content was mixed and when the exothermal reaction was completed (no further rise of temperature) the reactor was heated to a temperature of 50 C and maintained at this temperature until all polyol was reacted (until the content of free isocyanate as measured according to ASTM D2572-19 was equal to the isocyanate content that could theoretically be achieved). This was typically after 1.5 to 2 hours. The reactor was then cooled to room temperature and the resulting prepolymer was collected from the reactor. The molecular weight and the free isocyanate content of the prepolymer thus prepared were determined.
Preparation of adhesive compositions Adhesive compositions were prepared by adding 0.2 wt% curing catalyst (JeffcatTM
DMDEE), 0.05 wt% defoaming agent (FoamasterTM MO 2115) and 0.8 wt% thickener (CarbosilTM TS 720) to the prepolymer. Methyl diphenyl diisocyanate (SuprasecTM
2004) was added until a content of free isocyanate groups between 14.5 and 16.5 wt% based on the total weight of the adhesive composition was achieved.
Test methods Longitudinal tensile shear strength With each adhesive composition, assemblies of beech panels were prepared according to EN302-1:2013 with a thick glue line (0.5 mm gap-joint). The amount of adhesive composition applied was in excess (double-sided application). The time between glue-up and testing was 13 days (at 65% relative humidity and 20 C).
The assembly time was approximately 4 min, the pressing time was 16 hours and the applied pressure was 8.0 kg/cm2.
The longitudinal tensile shear strength of bonded assemblies with thick glue lines was determined after treatment A4 as described in EN302-1: 2013: A4: Soaking in boiling water for 6 hours, following by soaking in cold water (20 C) for 2 hours. The samples were tested in the wet state.
Date Recue/Date Received 2024-03-11
Preparation of adhesive compositions Adhesive compositions were prepared by adding 0.2 wt% curing catalyst (JeffcatTM
DMDEE), 0.05 wt% defoaming agent (FoamasterTM MO 2115) and 0.8 wt% thickener (CarbosilTM TS 720) to the prepolymer. Methyl diphenyl diisocyanate (SuprasecTM
2004) was added until a content of free isocyanate groups between 14.5 and 16.5 wt% based on the total weight of the adhesive composition was achieved.
Test methods Longitudinal tensile shear strength With each adhesive composition, assemblies of beech panels were prepared according to EN302-1:2013 with a thick glue line (0.5 mm gap-joint). The amount of adhesive composition applied was in excess (double-sided application). The time between glue-up and testing was 13 days (at 65% relative humidity and 20 C).
The assembly time was approximately 4 min, the pressing time was 16 hours and the applied pressure was 8.0 kg/cm2.
The longitudinal tensile shear strength of bonded assemblies with thick glue lines was determined after treatment A4 as described in EN302-1: 2013: A4: Soaking in boiling water for 6 hours, following by soaking in cold water (20 C) for 2 hours. The samples were tested in the wet state.
Date Recue/Date Received 2024-03-11
14 Closed assembly time (AT) Closed assembly time of the adhesive compositions was determined according to EN14080:2013.
With each adhesive composition, assemblies were prepared by gluing together five lamellas of spruce, with the dimensions of 285x145x30mm. The amount of adhesive composition applied was 120g/m2. The lamellas were assembled into a stack directly after the application of the adhesive composition. After different time intervals (assembly times), the assemblies were pressed for 16 hours. The applied pressure was 8.0 kg/cm2.
After 5 days at 20 C and 65% relative humidity, delamination of the glue line was determined according to Annex C of EN14080:2013, using method B.
Closed assembly time is the longest assembly time that can be applied without exceeding the delamination value in Table 9 of EN14080:2013.
Minimum pressing time (PT) The minimum pressing time of the adhesive compositions was determined was determined according to EN14080:2013.
With each adhesive composition, assemblies were prepared by gluing together five lamellas of spruce, with the dimensions of 285x145x30mm. The amount of adhesive composition applied was 120g/m2. After 2 minutes assembly time, the assemblies were pressed with an applied pressure of 8kg/cm2. The press times were varied.
After 5 days at 20 C and 65% relative humidity, delamination of the glue line was determined according to Annex C of EN14080:2013, using method B.
Minimum pressing time is the minimum pressing time needed without exceeding the
With each adhesive composition, assemblies were prepared by gluing together five lamellas of spruce, with the dimensions of 285x145x30mm. The amount of adhesive composition applied was 120g/m2. The lamellas were assembled into a stack directly after the application of the adhesive composition. After different time intervals (assembly times), the assemblies were pressed for 16 hours. The applied pressure was 8.0 kg/cm2.
After 5 days at 20 C and 65% relative humidity, delamination of the glue line was determined according to Annex C of EN14080:2013, using method B.
Closed assembly time is the longest assembly time that can be applied without exceeding the delamination value in Table 9 of EN14080:2013.
Minimum pressing time (PT) The minimum pressing time of the adhesive compositions was determined was determined according to EN14080:2013.
With each adhesive composition, assemblies were prepared by gluing together five lamellas of spruce, with the dimensions of 285x145x30mm. The amount of adhesive composition applied was 120g/m2. After 2 minutes assembly time, the assemblies were pressed with an applied pressure of 8kg/cm2. The press times were varied.
After 5 days at 20 C and 65% relative humidity, delamination of the glue line was determined according to Annex C of EN14080:2013, using method B.
Minimum pressing time is the minimum pressing time needed without exceeding the
15 delamination value in Table 9 of EN14080:2013.
The longitudinal tensile shear strength, AT and PT are shown in Table 2.
Table 2 Prepolymers and adhesive compositions: ingredients and properties 1 2* 3* 4* 5* 6* 7*
wt% eq.a wt% eq.a wt% eq.a wt% eq.a wt% eq.a wt% eq.a wt% eq.a Polyisocyanate mixture (a) Suprasec TM 47 4.0 39 4.3 26 2.85 55 5.0 51 5.0 46 4.0 47 5.0 SuprasecTM 12 1.0 14 1.4 26 2.85 - 11 1.0 Polyol mixture (b) PolyTHFTM 21 0.45 21 0.6 20 0.6 25 0.5 23 0.5 25 0.5 22 0.6 VoranolTM 12 0.45 16 0.4 13 0.4 18 0.5 LupranolTM 8 0.10 26 0.4 28 0.4 4 0.1 - 31 0.4 LupranolTM 2095 13 0.1 Total wt% 100 100 100 100 100 100 Mn (g/mol) 509 419 455 Mw (g/mol) 3211 2848 2792 NCO content 15.2 15.0 15.4 12.8 prepolymer (wt%) NCO content 16.1 14.5 15 15.8 15.6 16 15.8 adhesive composition (wt%) AT/PT 1:1.6 1:2.7 1:1 1:2 1:2.5 1:2.5 1:1.5 AT (minutes) 5 3 10 5 8 5 10 PT (minutes) 8 8 10 10 20 12.5 15 Shear strength 5.34 5.27 2.61 4.66 4.9 5.69 2.6 (MPa) * comparison examples a equivalents NCO or OH
AT: closed assembly time PT: minimum pressing time The examples show that an adhesive composition with a prepolymer prepared by reacting a polyisocyanate comprising uretonimine-modified MDI and a polyol mixture comprising poly(tetrahydrofuran), a triol with secondary hydroxyl groups and an amine-initiated polyether Date Recue/Date Received 2024-03-11
The longitudinal tensile shear strength, AT and PT are shown in Table 2.
Table 2 Prepolymers and adhesive compositions: ingredients and properties 1 2* 3* 4* 5* 6* 7*
wt% eq.a wt% eq.a wt% eq.a wt% eq.a wt% eq.a wt% eq.a wt% eq.a Polyisocyanate mixture (a) Suprasec TM 47 4.0 39 4.3 26 2.85 55 5.0 51 5.0 46 4.0 47 5.0 SuprasecTM 12 1.0 14 1.4 26 2.85 - 11 1.0 Polyol mixture (b) PolyTHFTM 21 0.45 21 0.6 20 0.6 25 0.5 23 0.5 25 0.5 22 0.6 VoranolTM 12 0.45 16 0.4 13 0.4 18 0.5 LupranolTM 8 0.10 26 0.4 28 0.4 4 0.1 - 31 0.4 LupranolTM 2095 13 0.1 Total wt% 100 100 100 100 100 100 Mn (g/mol) 509 419 455 Mw (g/mol) 3211 2848 2792 NCO content 15.2 15.0 15.4 12.8 prepolymer (wt%) NCO content 16.1 14.5 15 15.8 15.6 16 15.8 adhesive composition (wt%) AT/PT 1:1.6 1:2.7 1:1 1:2 1:2.5 1:2.5 1:1.5 AT (minutes) 5 3 10 5 8 5 10 PT (minutes) 8 8 10 10 20 12.5 15 Shear strength 5.34 5.27 2.61 4.66 4.9 5.69 2.6 (MPa) * comparison examples a equivalents NCO or OH
AT: closed assembly time PT: minimum pressing time The examples show that an adhesive composition with a prepolymer prepared by reacting a polyisocyanate comprising uretonimine-modified MDI and a polyol mixture comprising poly(tetrahydrofuran), a triol with secondary hydroxyl groups and an amine-initiated polyether Date Recue/Date Received 2024-03-11
16 dial has a very good AT/PT ratio (between 1:1 and 1:2) and provides bonds with very good shear strength.
Claims (20)
1. A one-component moisture-curing adhesive composition comprising from 80 to 100 wt% of an isocyanate-functional prepolymer obtainable by reacting:
(a) a polyisocyanates mixture having an average nominal isocyanate functionality in the range of from above 2.00 to below 2.05 comprising:
(al) a diisocyanate comprising methyl diphenyl diisocyanate; and (a2) an uretonimine-modified methyl diphenyl diisocyanate comprising at least isocyanate functional groups; and (b) a polyol mixture comprising:
(bl) a linear butylene oxide-based diol with two primary hydroxyl groups;
(b2) a polyether triol with three secondary hydroxyl groups; and (b3) an amine-initiated polyether polyol;
wherein the equivalent ratio between isocyanate groups in (a) and hydroxyl groups in (b) is in the range of from 3.5 to 7.0, wherein the content of free isocyanate groups in the adhesive composition is in the range of from 14 to 17 wt% determined according to ASTM D2572-19, and wherein polyisocyanates mixture (a) comprises diisocyanate (al) in excess of uretomine-modified methyl diphenyl diisocyanate (a2).
(a) a polyisocyanates mixture having an average nominal isocyanate functionality in the range of from above 2.00 to below 2.05 comprising:
(al) a diisocyanate comprising methyl diphenyl diisocyanate; and (a2) an uretonimine-modified methyl diphenyl diisocyanate comprising at least isocyanate functional groups; and (b) a polyol mixture comprising:
(bl) a linear butylene oxide-based diol with two primary hydroxyl groups;
(b2) a polyether triol with three secondary hydroxyl groups; and (b3) an amine-initiated polyether polyol;
wherein the equivalent ratio between isocyanate groups in (a) and hydroxyl groups in (b) is in the range of from 3.5 to 7.0, wherein the content of free isocyanate groups in the adhesive composition is in the range of from 14 to 17 wt% determined according to ASTM D2572-19, and wherein polyisocyanates mixture (a) comprises diisocyanate (al) in excess of uretomine-modified methyl diphenyl diisocyanate (a2).
2. A one-component moisture-curable adhesive composition according to claim 1, wherein butylene oxide-based diol (bl) has a number average molecular weight in the range of from 500 to 1,500 g/mol determined by size-exclusion chromatography using polystyrene standards according to ISO 16014-1.
3. A one-component moisture-curable adhesive composition according to claim 1 or 2, wherein polyether triol (b2) has a number average molecular weight in the range of from 500 to 1,500 g/mol determined by size-exclusion chromatography using polystyrene standards according to ISO 16014-1.
4. A one-component moisture-curable adhesive composition according to any one of claims 1 to 3, wherein the polyol mixture (b) is substantially free of any polyols other than (bl), (b2) and (b3).
Date Recue/Date Received 2024-03-11
Date Recue/Date Received 2024-03-11
5. A one-component moisture-curable adhesive composition according to any one of claims 1 to 4, wherein the equivalent ratio between isocyanate groups in (a) and hydroxyl groups in (b) is in the range of from 4.0 to 6.5.
6. A one-component moisture-curable adhesive composition according to any one of claims 1 to 5, wherein the equivalent ratio between isocyanate groups in (a) and hydroxyl groups in (b) is in the range of from 4.5 to 6Ø
7. A one-component moisture-curable adhesive composition according to any one of claims 1 to 6, wherein the content of free isocyanate groups in the adhesive composition is in the range of from 15.0 to 16.5 wt% determined according to ASTM
D2572-19.
D2572-19.
8. A one-component moisture-curable adhesive composition according to any one of claims 1 to 7, wherein the diisocyanate (al) is methyl diphenyl diisocyanate.
9. A one-component moisture-curable adhesive composition according to claim 8, wherein polyisocyanate mixture (a) essentially consists of methyl diphenyl diisocyanate and an uretonimine-modified methyl diphenyl diisocyanate.
10. A one-component moisture-curable adhesive composition according to any one of claims 1 to 9, wherein the uretonimine-modified diisocyanate (a2) comprises in the range of from 3 to 10 isocyanate functional groups.
11. A one-component moisture-curable adhesive composition according to any one of claims 1 to 10, wherein the uretonimine-modified diisocyanate (a2) comprises in the range of from 3 to 6 isocyanate functional groups.
12. A one-component moisture-curable adhesive composition according to any one of claims 1 to 11, wherein the uretonimine-modified diisocyanate (a2) comprises 3 or 4 isocyanate functional groups.
13. A one-component moisture-curable adhesive composition according to any one of claims 1 to 12, comprising from 85 to 99.8 wt% of the prepolymer.
Date Recue/Date Received 2024-03-11
Date Recue/Date Received 2024-03-11
14. A one-component moisture-curable adhesive composition according to any one of claims 1 to 13, further comprising a curing catalyst.
15. A one-component moisture-curable adhesive composition according to claim 14, wherein the curing catalyst is 2,2'-dimorpholinediethylether.
16. A one-component moisture-curable adhesive composition according to any one of claims 1 to 15, further comprising one or more additives.
17. A one-component moisture-curable adhesive composition according to any one of claims 1 to 16, further comprising a defoaming agent and/or a thickener.
18. A method of bonding a first piece of material to a second piece of material, comprising contacting a surface of the first material with a surface of the second material, wherein at least one of the contacted surfaces has the adhesive composition according to any one of the claims 1 to 17 applied to it prior to the contacting.
19. An object comprising a first piece of material and a second piece of material bonded with the adhesive composition according to any one of claims 1 to 17.
20. An object according to claim 19, wherein the material is wood, and the object is a structural wood product.
Date Recue/Date Received 2024-03-11
Date Recue/Date Received 2024-03-11
Applications Claiming Priority (3)
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| EP21185300.7 | 2021-07-13 | ||
| EP21185300 | 2021-07-13 | ||
| PCT/EP2022/069663 WO2023285561A1 (en) | 2021-07-13 | 2022-07-13 | One-component moisture-curable adhesive composition |
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|---|---|
| CA3223825A1 CA3223825A1 (en) | 2023-01-19 |
| CA3223825C true CA3223825C (en) | 2024-05-07 |
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| CA3223825A Active CA3223825C (en) | 2021-07-13 | 2022-07-13 | One-component moisture-curable adhesive composition |
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| Country | Link |
|---|---|
| EP (1) | EP4370329A1 (en) |
| JP (1) | JP2024525541A (en) |
| CN (1) | CN117693427A (en) |
| AU (1) | AU2022310127B2 (en) |
| BR (1) | BR112023026346A2 (en) |
| CA (1) | CA3223825C (en) |
| CO (1) | CO2023017149A2 (en) |
| EC (1) | ECSP24010296A (en) |
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Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1999019141A1 (en) | 1997-10-10 | 1999-04-22 | Huntsman Ici Chemicals Llc | Polyisocyanate adhesive for plywood |
| DE19935489A1 (en) * | 1999-07-28 | 2001-02-08 | Basf Ag | Adhesive composition for finger jointing |
| DE10237649A1 (en) | 2001-08-16 | 2003-02-27 | Henkel Kgaa | A single coat rapid acting polyurethane adhesive useful as a coating-, sealing-, household-, assembly-, structural-, packaging-, or paper adhesive and for film coating |
| CA2485447A1 (en) * | 2002-02-08 | 2003-08-14 | Henkel Kommanditgesellschaft Auf Aktien | Neutral-coloured 1k polyurethane adhesive |
| JP2022549755A (en) | 2019-08-06 | 2022-11-29 | ダウ グローバル テクノロジーズ エルエルシー | One-component polyurethane prepolymer composition |
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2022
- 2022-07-13 JP JP2024500129A patent/JP2024525541A/en active Pending
- 2022-07-13 CA CA3223825A patent/CA3223825C/en active Active
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- 2022-07-13 WO PCT/EP2022/069663 patent/WO2023285561A1/en active Application Filing
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| CO2023017149A2 (en) | 2023-12-20 |
| ECSP24010296A (en) | 2024-03-01 |
| AU2022310127A1 (en) | 2024-01-18 |
| PE20240432A1 (en) | 2024-03-07 |
| AU2022310127B2 (en) | 2024-02-08 |
| WO2023285561A1 (en) | 2023-01-19 |
| BR112023026346A2 (en) | 2024-03-05 |
| CA3223825A1 (en) | 2023-01-19 |
| CN117693427A (en) | 2024-03-12 |
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